微波辐照对低阶煤的表面改性作用

以微波辐照作为低阶煤浮选前的预处理方法,研究微波辐照对低阶煤的表面改性作用。结果表明:微波辐照预处理显著提高了浮选精煤产率与可燃体回收率,在微波处理时间为15min时精煤产率和可燃体回收率达到了最高值,分别为74.56%,84.83%。微波辐照后煤样接触角有所增加,疏水性增强。红外光谱、质量损失与比表面积分析结果表明,存在于煤颗粒小孔中的水分子或者某些极性小分子在微波的作用下被加热去除,从而导致煤颗粒疏水性增强,提高了煤的可浮性。

Bio-solubilization of Chinese lignite I:extra-cellular protein analysis

A white rot fungus strain, Trichoderma sp.AH, was isolated from rotten wood in Fushun and used to study the mechanism of lignite bio-solubilization.The results showed that nitric acid pretreated Fushun lignite was solubilized by T.sp.AH and that extracellular proteins from T.sp.AH were correlated with the lignite bio-solubilization results.In the presence of Fushun lignite the extracellular protein concentration from T.sp.AH was 4.5 g/L while the concentration was 3 g/L in the absence of Fushun lignite.Sodium dodecyl sulfate polyacrylamide gel electrophoresis(SDS-PAGE) of the extracellular proteins detected at least four new protein bands after the T.sp.AH had solubilized the lignite.Enzyme color reactions showed that extracellular proteins from T.sp.AH mainly consisted of phenol-oxidases, but that lignin decomposition enzymes such as laccase, peroxidase and manganese peroxidases were not present.

Bio-solubilization of Chinese lignite II:protein adsorption onto the lignite surface

Lignite bio-solubilization is a promising technology for converting solid lignite into oil.This study concerns the adsorption of lignite-solubilizing enzymes onto the lignite surface.Adsorption capacity, infrared spectral analysis and driving forces analysis are studied as a way to help understand the bio-solubilization mechanism.The results show that the amount of lignite bio-solubilization is proportional to the amount of adsorbed lignite-solubilizing enzymes.An increase in lignite-solubilizing enzyme adsorption of 10% leads to a 7% increase in lignite bio-solubilization.However, limited amounts of enzymes can be adsorbed by the lignite, thus resulting in low percentages of bio-solubilization.Infrared spectral analysis shows that side chains, such as hy-droxyl and carbonyl, of the lignite structure are the main, and necessary, structures where lignite-solubilizing enzymes attachto the lignite.Furthermore, driving force analysis indicates that the electrostatic force between lignite and enzymes is the main adsorption mechanism.The forces are influenced by solution pH levels, the zeta potential of the lignite and the isoelectric points of the en-zymes.

Low Density Dry Coal Beneficiation Using an Air Dense Medium Fluidized Bed

For the production of low ash content clean coal, separation at low density is required for some raw coals.Based on analyzing the fluidizing characteristics of magnetic-pearls with a specific size clistribution and formation mechanism of a microbubble fluidized bed, optimal technological and operating parameters suitable for low density coal separation were determined. The experimental results show that an air dense medium fluidized bed with low den-sity can be formed using magnetic pearls as medium solids, which can efficiently beneficiate coal of 6-50 mm size with a probable error Ep value of 0.05 at a separating density of 1.44 g/cm^3.

Mechanism of oxidation of low rank coal by nitric acid

The pretreatment of low rank coal with nitric acid oxidation can promote its bio-liquefaction. However, the detailed mechanism of which remains an unresolved problem. In the present work, the characteristics of Fushun coal before and after oxidation by nitric acid were investigated combined with elemental composition, pore volume and pore size, Zeta potential, FT-IR, and 13C solid NMR spectrum analysis. The results show that the inorganic substance inlaid in coal are dissolved by ni- tric acid, which results in the decrease of coal ash content and increase of pore volume and pore size. Furthermore, there exist obvious chemical reactions between nitric acid and the functional groups of coal including aromatic ring carboxylation, side chain alkyl of aromatic ring oxidation and aromatic ring nitration. Among these reactions, some led to the increase in content of carboxyl, aliphatic carbon connected with O and humic acid carbon, while others caused the reduction of aromaticity, methyl carbon, substituted aryl carbon and side chain.